BDBM50217328 CHEMBL268513

SMILES: CCCc1c([nH]c2ccc(CC(O)=O)cc12)-c1ccccc1

InChI Key: InChIKey=KTUCGDFKCLFWOU-UHFFFAOYSA-N

Data: 1 KI  1 EC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50217328   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Peroxisome proliferator-activated receptor (Homo sapiens (Human))	BDBM50217328 (CHEMBL268513) Show SMILES CCCc1c([nH]c2ccc(CC(O)=O)cc12)-c1ccccc1 Show InChI InChI=1S/C19H19NO2/c1-2-6-15-16-11-13(12-18(21)22)9-10-17(16)20-19(15)14-7-4-3-5-8-14/h3-5,7-11,20H,2,6,12H2,1H3,(H,21,22)	PDB MMDB NCI pathway Reactome pathway KEGG B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.89E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Wellcome Research and Development Curated by ChEMBL					Assay Description Binding affinity against Peroxisome proliferator activated receptor gamma (PPAR gamma)				Bioorg Med Chem Lett 9: 3329-34 (2000) BindingDB Entry DOI: 10.7270/Q2FN15FG
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor (Homo sapiens (Human))	BDBM50217328 (CHEMBL268513) Show SMILES CCCc1c([nH]c2ccc(CC(O)=O)cc12)-c1ccccc1 Show InChI InChI=1S/C19H19NO2/c1-2-6-15-16-11-13(12-18(21)22)9-10-17(16)20-19(15)14-7-4-3-5-8-14/h3-5,7-11,20H,2,6,12H2,1H3,(H,21,22)	PDB MMDB NCI pathway Reactome pathway KEGG B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	7.08E+3	n/a	n/a	n/a	n/a
Glaxo Wellcome Research and Development Curated by ChEMBL					Assay Description Transcriptional activation of peroxisome proliferator activated receptor gamma				Bioorg Med Chem Lett 9: 3329-34 (2000) BindingDB Entry DOI: 10.7270/Q2FN15FG
					More data for this Ligand-Target Pair